Double Lumen Tube Intubation (DLETI)

International Institute of Rescue Research and Education

Status: Unknown

Conditions: Endotracheal Intubation; Cardiac Arrest

Treatments: Device: standard double-lumen tube; Device: VivaSight Double Lumen Tube

Study type: Interventional

Funder types: Other

Identifiers

NCT02295657

ETI/2014/43

Details and patient eligibility

About

The aim of this study was to compare time, success rates of different double-lumen tubes in intubation in a standardized manikin model.

Enrollment: 120 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• give voluntary consent to participate in the study
• minimum 1 year of work experience in emergency medicine
• experienced emergency medicine personnel (physicians, nurses, paramedics)

Exclusion criteria

• not meet the above criteria
• wrist or low back diseases

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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120 participants in 1 patient group

ETI intubation

Experimental group

Description:

endotracheal intubation in manikin

Treatment:

Device: standard double-lumen tube

Device: VivaSight Double Lumen Tube